| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001282726.1 | 965 | Missense Mutation | CCT,CTT | P217L | NP_001269655.1 |
| NM_001282727.1 | 965 | Missense Mutation | CCT,CTT | P181L | NP_001269656.1 |
| NM_006358.3 | 965 | Missense Mutation | CCT,CTT | P254L | NP_006349.1 |